Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study

OBJECTIVE: Dravet syndrome or severe myoclonic epilepsy of infancy (SMEI) is a baleful epileptic encephalopathy that begins in the first year of life. This syndrome specified by febrile seizures followed by intractable epilepsy, disturbed psychomotor development, and ataxia. Clinical similarities be...

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Bibliografiset tiedot
Päätekijät: TONEKABONI, Seyed Hassan, EBRAHIMI, Ahmad, BAKHSHANDEH BALI, Mohammad Kazem, TAHERI OTAGHSARA, Seyedeh Mohadeseh, HOUSHMAND, Massoud, NASEHI, Mohammad Mahdi, TAGHDIRI, Mohammad Mahdi, MOGHADDASI, Mehdi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Shahid Beheshti University of Medical Sciences 2013
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3943035/
https://ncbi.nlm.nih.gov/pubmed/24665294
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